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Akkodis · 1 day ago

Data Scientist

Novato, CA

Contract

Onsite

Mid, Senior Level

$70/hr - $75/hr

3+ years exp

Akkodis is seeking a Data Scientist for a Contract job with a client. The role focuses on supporting central monitoring and risk-based quality management for clinical trials, implementing and running risk metrics using clinical data with an emphasis on SAS programming.

Information Technology & Services

H1B Sponsor Likely

Hiring Manager

Prakhar G.

Responsibilities

Implement and maintain pre-defined KRIs, QTLs, and triggers using robust SAS programs/macros across multiple clinical studies

Extract, transform, and integrate data from EDC systems (e.g., RAVE) and other clinical sources into analysis-ready SAS datasets

Run routine and ad-hoc RBQM/central monitoring outputs (tables, listings, data extracts, dashboard feeds) to support signal detection and study review

Perform QC and troubleshooting of SAS code; ensure outputs are accurate and efficient

Maintain clear technical documentation (specifications, validation records, change logs) for all RBQM programs and processes

Collaborate with Central Monitors, Central Statistical Monitors, Data Management, Biostatistics, and Study Operations to understand requirements and ensure correct implementation of RBQM metrics

Qualification

Advanced SAS programmingClinical trial data experienceRAVE EDCCDISC standards knowledgeAnalytical skillsProblem-solving skillsCommunication skillsTeamwork skillsTime management

Required

PhD, MS, or BA/BS in statistics, biostatistics, computer science, data science, life science, or a related field

Relevant clinical development experience (programming, RBM/RBQM, Data Management), for example: PhD: 3+ years, MS: 5+ years, BA/BS: 8+ years

Advanced SAS programming skills (hard requirement) in a clinical trials environment (Base SAS, Macro, SAS SQL; experience with large, complex clinical datasets)

Hands-on experience working with clinical trial data

Proficiency with Microsoft Word, Excel, and PowerPoint

Knowledge of GCP, ICH, FDA guidance related to clinical trials and risk-based monitoring

Strong analytical and problem-solving skills; ability to interpret complex data and risk outputs

Effective communication and teamwork skills; comfortable collaborating with cross-functional, global teams

Ability to manage multiple programming tasks and deliver high-quality work in a fast-paced environment

Preferred

Experience with RAVE EDC

Awareness or working knowledge of CDISC, CDASH, SDTM standards

Exposure to R, Python, or JavaScript and/or clinical data visualization tools/platforms

Benefits

Medical

Dental

Vision

Life insurance

Short-term disability

Additional voluntary benefits

An EAP program

Commuter benefits

401K plan

Paid Sick Leave

Holiday pay

Company

Akkodis

Glassdoor3.3

Akkodis provides digital engineering solutions for sustainable and innovative industries.

Zug, Zug, CHE

10001+ employees

https://www.akkodis.com

H1B Sponsorship

Akkodis has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)

Distribution of Different Job Fields Receiving Sponsorship

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Trends of Total Sponsorships

2025 (141)

2024 (121)

2023 (67)